BEKLYN ABSOLUTE PURIFYING-SPRAY- titanium dioxide, hypochlorous acid liquid

Beklyn Absolute Purifying-Spray by

Drug Labeling and Warnings

Beklyn Absolute Purifying-Spray by is a Otc medication manufactured, distributed, or labeled by MY Corp.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

titanium dioxide, hypochlorous acid

INACTIVE INGREDIENT

Foeniculum Vulgare Fruit Extract, Maltitol, Polygonum Tinctorium Leaf Extract, Sorbitol, Water

PURPOSE

Hand sanitizer to help reduce bacteria that potentially can cause disease. Recommended for repeated use

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

• Spray directly, from a distance of about 8 to 10 inches and rub hands together until dry.
• For children under 6 years use adult supervision
• Not recommended for infants

WARNINGS

For external use only. 

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs develop and persist for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BEKLYN ABSOLUTE PURIFYING-SPRAY 
titanium dioxide, hypochlorous acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71544-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	0.03 g  in 300 mL
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10)	HYPOCHLOROUS ACID	0.024 g  in 300 mL

Inactive Ingredients
Ingredient Name	Strength
FOENICULUM VULGARE FRUIT (UNII: J5W36Y5WG8)
MALTITOL (UNII: D65DG142WK)
PERSICARIA TINCTORIA LEAF (UNII: FU6582QMPV)
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71544-0002-1	300 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/15/2020

Labeler - MY Corp.,Ltd (688202781)

Registrant - MY Corp.,Ltd (688202781)

Establishment
Name	Address	ID/FEI	Business Operations
MY Corp.,Ltd		688202781	manufacture(71544-0002) , label(71544-0002) , pack(71544-0002)